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High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma

Histopathology, 2006-04, Vol.48 (5), p.579-587

2006

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Two populations of double minute chromosomes harbor distinct amplicons, the MYC locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line

Cytogenetic and genome research, 2009-01, Vol.124 (1), p.1-11

2009

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Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system

Histopathology, 2005-12, Vol.47 (6), p.631-637

2005

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Neurofibromatosis 1 (NF1) mRNAs expressed in the central nervous system are differentially spliced in the 5′ part of the gene

Human molecular genetics, 1995-05, Vol.4 (5), p.915-920

1995

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Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

The New England journal of medicine, 1999-06, Vol.340 (25), p.1954-1961

1999

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MYCN-non-amplified metastatic neuroblastoma with good prognosis and spontaneous regression: A molecular portrait of stage 4S

Molecular oncology, 2008-10, Vol.2 (3), p.261-271

2008

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Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

Genes chromosomes & cancer, 1997-01, Vol.18 (1), p.59-65

1997

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Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH

Nucleic acids research, 2004-01, Vol.32 (13), p.e112-e112

2004

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Tissue-specific alternative splicing of neurofibromatosis 1 (NF1) mRNA

Biomedicine & pharmacotherapy, 1994, Vol.48 (8), p.365-372

1994

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MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14)

Cytogenetic and genome research, 1996-01, Vol.73 (4), p.325-330

1996

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Assignment of the NTRK4 (trkE) gene to chromosome 6p21

Human genetics, 1996-07, Vol.98 (1), p.12-15

1996

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High frequency trans-splicing in a cell line producing spliced and polyadenylated RNA polymerase I transcripts from an rDNA-myc chimeric gene

Nucleic acids research, 2005-01, Vol.33 (7), p.2332-2342

2005

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Mapping of the 7q31 subregion common to the small chromosome 7 derivatives from two sporadic papillary renal cell carcinomas : increased copy number and overexpression of the MET proto-oncogene

Oncogene, 2000-02, Vol.19 (6), p.754-761

2000

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Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization

Human genetics, 1991-11, Vol.88 (1), p.21-26

1991

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Comparative genomic hybridization analysis of sporadic neuroendocrine tumors of the digestive system

Genes chromosomes & cancer, 1998-05, Vol.22 (1), p.50-56

1998

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The neurofibromatosis 1 gene transcripts expressed in peripheral nerve and neurofibromas bear the additional exon located in the GAP domain

Biochemical and biophysical research communications, 1992-10, Vol.188 (2), p.851-857

1992

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Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas

Genes chromosomes & cancer, 1996-11, Vol.17 (3), p.156-165

1996

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Emergence and Scattering of Multiple Neurofibromatosis (NF1)-Related Sequences During Hominoid Evolution Suggest a Process of Pericentromeric Interchromosomal Transposition

Human molecular genetics, 1997-01, Vol.6 (1), p.9-16

1997

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Mapping of the Tyrosine Kinase Receptors trkA (NTRK1), trkB (NTRK2) and trkC (NTRK3) to Human Chromosomes 1q22,9q22 and 15q25 by Fluorescence in situ Hybridization

European journal of human genetics : EJHG, 1997-03, Vol.5 (2), p.102-104

1997

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PTEN and DMBT1 homozygous deletion and expression in medulloblastomas and supratentorial primitive neuroectodermal tumors

Oncology reports, 2004-12, Vol.12 (6), p.1341

2004

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Chromosomal abnormalities in human glioblastomas: Gain in chromosome 7p correlating with loss in chromosome 10q

Molecular carcinogenesis, 2003-01, Vol.36 (1), p.6-14

2003

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Duplication of the Ph-chromosome as a possible mechanism of resistance to imatinib mesylate in patients with chronic myelogenous leukemia

Cancer genetics and cytogenetics, 2005-12, Vol.163 (2), p.189-190

2005

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A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level

Human genetics, 1995-07, Vol.96 (1), p.131-132

1995

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A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allow the identification of both alleles at the mRNA level

Human genetics, 1995, Vol.96 (1), p.131-132

1995

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Emergence and scattering of multiple neurobibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition

Human molecular genetics, 1997, Vol.6 (1), p.9-16

1997

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High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma

Two populations of double minute chromosomes harbor distinct amplicons, the MYC locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line

Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system

Neurofibromatosis 1 (NF1) mRNAs expressed in the central nervous system are differentially spliced in the 5′ part of the gene

Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

MYCN-non-amplified metastatic neuroblastoma with good prognosis and spontaneous regression: A molecular portrait of stage 4S

Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH

Tissue-specific alternative splicing of neurofibromatosis 1 (NF1) mRNA

MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14)

Assignment of the NTRK4 (trkE) gene to chromosome 6p21

High frequency trans-splicing in a cell line producing spliced and polyadenylated RNA polymerase I transcripts from an rDNA-myc chimeric gene

Mapping of the 7q31 subregion common to the small chromosome 7 derivatives from two sporadic papillary renal cell carcinomas : increased copy number and overexpression of the MET proto-oncogene

Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization

Comparative genomic hybridization analysis of sporadic neuroendocrine tumors of the digestive system

The neurofibromatosis 1 gene transcripts expressed in peripheral nerve and neurofibromas bear the additional exon located in the GAP domain

Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas

Emergence and Scattering of Multiple Neurofibromatosis (NF1)-Related Sequences During Hominoid Evolution Suggest a Process of Pericentromeric Interchromosomal Transposition

Mapping of the Tyrosine Kinase Receptors trkA (NTRK1), trkB (NTRK2) and trkC (NTRK3) to Human Chromosomes 1q22,9q22 and 15q25 by Fluorescence in situ Hybridization

PTEN and DMBT1 homozygous deletion and expression in medulloblastomas and supratentorial primitive neuroectodermal tumors

Chromosomal abnormalities in human glioblastomas: Gain in chromosome 7p correlating with loss in chromosome 10q

Duplication of the Ph-chromosome as a possible mechanism of resistance to imatinib mesylate in patients with chronic myelogenous leukemia

A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level

A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allow the identification of both alleles at the mRNA level

Emergence and scattering of multiple neurobibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition

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